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Results 1 - 10 of 25 for Sensory neuropathy
  1. SPTLC1 gene 
    ... SPTLC1 gene have been found to cause hereditary sensory neuropathy type IA. This condition is characterized by nerve ... sensation and muscle weakness in people with hereditary sensory neuropathy type IA. More About This Health Condition MedlinePlus ...
    https://medlineplus.gov/genetics/gene/sptlc1 - Genetics
  2. DNMT1 gene 
    ... tingling, or pain in the arms and legs (sensory neuropathy) can also occur. Affected individuals usually survive into ... above), people with HSAN IE have sensorineural deafness, sensory neuropathy, cognitive decline, and a shortened lifespan. However, they ...
    https://medlineplus.gov/genetics/gene/dnmt1 - Genetics
  3. ATL1 gene 
    ... been found to cause a condition called hereditary sensory neuropathy type ID. This condition is characterized by nerve ... gene mutations have been found to cause hereditary sensory neuropathy type ID. These mutations impair nerve cell function ...
    https://medlineplus.gov/genetics/gene/atl1 - Genetics
  4. SLC12A6 gene 
    ... used for muscle movement and sensation (motor and sensory neuropathy). Almost all affected individuals of French-Canadian descent ... JP, Carpenter S, Rouleau GA. Hereditary motor and sensory neuropathy with agenesis of the corpus callosum. Ann Neurol. ...
    https://medlineplus.gov/genetics/gene/slc12a6 - Genetics
  5. RETREG1 gene 
    ... Reilly MM. Mutation in FAM134B causing severe hereditary sensory neuropathy. J Neurol Neurosurg Psychiatry. 2012 Jan;83(1): ... Jonghe P, Timmerman V. Disease mechanisms in hereditary sensory and autonomic neuropathies. Neurobiol Dis. 2006 Feb;21(2):247-55. ...
    https://medlineplus.gov/genetics/gene/retreg1 - Genetics
  6. WNK1 gene 
    ... system--specific HSN2 exon of WNK1 cause hereditary sensory neuropathy type II. J Clin Invest. 2008 Jul;118( ... Jonghe P, Timmerman V. Disease mechanisms in hereditary sensory and autonomic neuropathies. Neurobiol Dis. 2006 Feb;21(2):247-55. ...
    https://medlineplus.gov/genetics/gene/wnk1 - Genetics
  7. VRK1 gene 
    ... described as a form of hereditary motor and sensory neuropathy (HMSN). HMSNs are a group of disorders that ... Mutations in VRK1 associated with complex motor and sensory axonal neuropathy plus microcephaly. JAMA Neurol. 2013 Dec;70(12): ...
    https://medlineplus.gov/genetics/gene/vrk1 - Genetics
  8. NGF gene 
    ... NGF: a "painless" NGF mutant, linked to hereditary sensory autonomic neuropathy type V, with full neurotrophic activity. PLoS One. ... Jonghe P, Timmerman V. Disease mechanisms in hereditary sensory and autonomic neuropathies. Neurobiol Dis. 2006 Feb;21(2):247-55. ...
    https://medlineplus.gov/genetics/gene/ngf - Genetics
  9. MFN2 gene 
    ... This variant is also called hereditary motor and sensory neuropathy VI.) Vision loss is caused by the breakdown ... mitochondrial assembly regulatory factor Tests of MFN2 PubMed NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIA, WITH OPTIC ATROPHY; HMSN6A MITOFUSIN 2; ...
    https://medlineplus.gov/genetics/gene/mfn2 - Genetics
  10. DHH gene 
    ... A, Tate G, Umehara F. Hereditary motor and sensory neuropathy with minifascicle formation in a patient with 46XY ...
    https://medlineplus.gov/genetics/gene/dhh - Genetics
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